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A Study Comparing Valsartan With And Without Hydrochlorothiazide In Patients With Hypertension

NCT ID: NCT00241007

Last Updated: 2011-11-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

836 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-12-31

Study Completion Date

2005-03-31

Brief Summary

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SAFETY EXTENSION STUDY TO THE CORE STUDY CVAH631C2301

Detailed Description

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Conditions

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Hypertension

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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VALSARTAN, VALSARTAN+HYDROCHLOROTHIAZIDE

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

SUCCESSFUL COMPLETION OF STUDY CVAH631C2301

\-

Exclusion Criteria

* NONE
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Novartis

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Novartis Pharmaceuticals

Role: STUDY_CHAIR

Novartis Pharmaceuticals

Locations

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Novartis Pharmaceuticals

East Hanover, New Jersey, United States

Site Status

Countries

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United States

Other Identifiers

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CVAH631C2301E1

Identifier Type: -

Identifier Source: org_study_id